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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT01839760
Registration number
NCT01839760
Ethics application status
Date submitted
8/04/2013
Date registered
25/04/2013
Date last updated
22/08/2014
Titles & IDs
Public title
Evaluation of Viral Shedding Patterns and Clinical Outcomes of Influenza Patients
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Scientific title
Prospective Study to Evaluate Viral Shedding Patterns and Clinical Outcomes of Hospitalized Adult Influenza Patients
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Secondary ID [1]
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FLU-EPI-001
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Influenza
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Condition category
Condition code
Intervention/exposure
Study type
Observational
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Patient registry
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
Inpatient cohort - Patients admitted to general wards
ICU cohort - Patients admitted to ICU
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Viral load/Viral shedding
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Assessment method [1]
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Outcome is the decay rate in viral load during hospital stay measured by quantitative polymerase chain reaction (QPCR)
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Timepoint [1]
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Day 7
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Primary outcome [2]
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Viral load/Viral shedding
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Assessment method [2]
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Outcome is the decay rate in viral load during hospital stay measured by quantitative polymerase chain reaction (QPCR)
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Timepoint [2]
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Day 9
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Primary outcome [3]
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Viral load/Viral shedding
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Assessment method [3]
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Outcome is the decay rate in viral load during hospital stay measured by quantitative polymerase chain reaction (QPCR)
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Timepoint [3]
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Day 11
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Primary outcome [4]
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Viral load/Viral shedding
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Assessment method [4]
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Outcome is the decay rate in viral load during hospital stay measured by quantitative polymerase chain reaction (QPCR)
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Timepoint [4]
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Day 13
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Primary outcome [5]
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Viral load/Viral shedding
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Assessment method [5]
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Outcome is the decay rate in viral load during hospital stay measured by quantitative polymerase chain reaction (QPCR)
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Timepoint [5]
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Day 15
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Eligibility
Key inclusion criteria
* Written informed consent
* Hospitalized or admitted to ICU for influenza
* Age =18 years
* Laboratory confirmation of influenza A or B
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
* Informed consent not given
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Study design
Purpose
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Duration
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Selection
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Timing
Prospective
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
1/12/2012
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
1/01/2014
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Sample size
Target
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Accrual to date
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Final
150
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Recruitment in Australia
Recruitment state(s)
NSW,SA
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Recruitment hospital [1]
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Westmead Hospital - Westmead
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Recruitment hospital [2]
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Royal Adelaide Hospital - Adelaide
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Recruitment postcode(s) [1]
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2145 - Westmead
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Recruitment postcode(s) [2]
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5000 - Adelaide
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Recruitment outside Australia
Country [1]
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United States of America
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State/province [1]
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Illinois
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Country [2]
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Canada
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State/province [2]
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Ontario
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Funding & Sponsors
Primary sponsor type
Commercial sector/industry
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Name
Crucell Holland BV
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Address
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Country
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Ethics approval
Ethics application status
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Summary
Brief summary
The objective of the study is virological assessment (e.g., proportion of prolonged viral shedding, median days to viral clearance, and viral load) in laboratory-confirmed adult influenza patients admitted to the general ward and/or to the ICU and to assess the correlation with the clinical manifestations and prognosis.
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Trial website
https://clinicaltrials.gov/study/NCT01839760
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Address
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Address
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Country
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Phone
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Fax
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Email
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Contact person for scientific queries
No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
No documents have been uploaded by study researchers.
Results not provided in
https://clinicaltrials.gov/study/NCT01839760
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